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Serum levels of retinol-binding protein 4 and the risk of non-small cell lung cancer: A case-control study

机译:血清水平的视黄醇结合蛋白4和非小细胞肺癌的风险:一个病例对照研究

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Retinol binding protein 4 (RBP4), as an adipokine, has been identified to be associated with several types of cancer. However, no studies have assessed its effect on non-small cell lung cancer (NSCLC) risk. The objective of this study was to assess the association between serum RBP4 levels and the risk of NSCLC. A case-control study design was used to recruit 256 confirmed NSCLC cases and 256 age- and gender-matched healthy controls by frequency between August 2017 and January 2019. Serum RBP4 was measured using enzyme-linked immune absorbent assay before treatment. Unconditional logistic regression analysis was applied to estimate the odds ratio and 95% confidence interval (CI). Serum RBP4 level was significantly higher in NSCLC patients than those in the healthy control group (36.05 ± 8.28 vs 29.54 ± 7.71 μg/mL, P .05). Higher serum RBP4 level was associated with increased risk of NSCLC ( P trend = .001). Compare with those in the lowest tertile, the adjusted odds ratios were 1.85 (95% CIs 1.07–3.2) ( P = .029) for the second tertile and 2.18 (95% CIs 1.37–3.45) ( P = .001) for the highest tertile after adjusting for confounding variables. No interactions were observed after stratified analyses by body mass index and smoking status ( P for interaction: .584 and .357). Our study indicated that serum RBP4 level was positively related to the risk of NSCLC. Additional studies with prospective design are required to confirm this finding.
机译:已经鉴定了视黄醇结合蛋白4(RBP4)作为己岛,与若干类型的癌症有关。然而,没有评估其对非小细胞肺癌(NSCLC)风险的影响。本研究的目的是评估血清RBP4水平与NSCLC的风险之间的关联。案例对照研究设计用于招募256例确诊的NSCLC病例,2017年8月至2019年1月在2019年1月至2019年1月之间进行了256次和性别匹配的健康对照。使用在处理前使用酶联免疫吸收测量测量血清RBP4。应用无条件逻辑回归分析来估计差距和95%置信区间(CI)。 NSCLC患者的血清RBP4水平明显高于健康对照组(36.05±8.28 vs 29.54±7.71μg/ ml,P <.05)。更高的血清RBP4水平与NSCLC的风险增加有关(P趋势= .001)。与最低特性的比较,调整后的差距为1.85(95%CIS 1.07-3.2)(P = .029),用于第二条塔,2.18(95%CIS 1.37-3.45)(P = .001)调整混淆变量后的最高触角。通过体重指数和吸烟状态分层分析后没有观察到相互作用(P用于相互作用:.584和.357)。我们的研究表明,血清RBP4水平与NSCLC的风险正相关。需要进行前瞻性设计的其他研究来确认这一发现。

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